HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoic acid, 4-fluoro-, ethyl ester → Ethyl 4-(4-cyclobutylpiperazin-1-yl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoic acid, 4-fluoro-, ethyl ester | HCID 67976 | — |
| Reactant | 1-Cyclobutylpiperazine | HCID 4738602 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | Ethyl 4-(4-cyclobutylpiperazin-1-yl)benzoate | HCID 57440408 | 11.31% |
Reaction Conditions
| Temperature | 150 °C |
|---|
Reaction Steps
Ethyl 4-fluorobenzoate (0.225 mL, 1.53 mmol) and 1-cyclobutylpiperazine (0.430 g, 3.07 mmol) were taken up in DMA (3 mL) and sealed into a microwave tube. The reaction was heated to 150° C. for 90 mins in the microwave reactor and cooled to room temperature. The reaction was not complete, so it was reheated at 150° C. for a further 1 h. The reaction mixture was evaporated to dryness and the crude product purified by silica column chromatography, eluting with a gradient of 0-2.5% MeOH in DCM. Pure fractions were evaporated to dryness to afford ethyl 4-(4-cyclobutylpiperazin-1-yl)benzoate (0.050 g, 11.31%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07737149B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-6c3cf9423faf4786bc8b745bf2d949bb |
| Source note | uspto-grants-2010_06 |